HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyldimethyl((4-nitrobenzyl)oxy)silane → 4-Aminobenzyloxy-tert-butyldimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyldimethyl((4-nitrobenzyl)oxy)silane | HCID 11065418 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Aminobenzyloxy-tert-butyldimethylsilane | HCID 11075470 | 94.2% |
Reaction Steps
In ethanol (80 ml) was dissolved tert-butyldimethyl-4-nitrobenzyloxysilane (16.5 g), and to the mixture was added dried 5% palladium on carbon (0.83 g). Under hydrogen atmosphere, the mixture was stirred at room temperature under atmospheric pressure for 7.5 hours. The palladium was filtered off, and the filtrate was concentrated. The residue was separated and purified with column chromatography (ethyl acetate/hexane=1/4) to give 4-aminobenzyloxy-tert-butyldimethylsilane (13.8 g) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172061B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-146cb188867747b6912f13ae57baacf6 |
| Source note | uspto-grants-2001_01 |